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Q43109842-C7BB3AAC-91D9-4563-AF2F-09601F80D537
Q43109842-C7BB3AAC-91D9-4563-AF2F-09601F80D537
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43109842-C7BB3AAC-91D9-4563-AF2F-09601F80D537
A novel GLI3c.750delC truncation mutation in a multiplex Greig cephalopolysyndactyly syndrome family with an unusual phenotypic combination in a patient.
P2860
Q43109842-C7BB3AAC-91D9-4563-AF2F-09601F80D537
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43109842-C7BB3AAC-91D9-4563-AF2F-09601F80D537
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
abf0b2177ea0af1f2134ec40ec8c5364d53b5c9d
P2860
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.